Clinical Trials · NCT04747392

Bioequivalence Study of SAL001 and FORSTEO in Healthy Chinese Adults

CompletedPhase 1Teriparatide (Approved)
Phase
Phase 1
Recruitment status
Completed
Sponsor
Shenzhen Salubris Pharmaceuticals Co., Ltd.
Enrollment
64
Start date
Aug 2020
Locations
1 site, China
Primary endpoint
PK parameters: area under the plasma concentration time curve from-time zero to time t (AUC0-t)
View Teriparatide compound reference